Canonical Allele Identifier: CA1737344136
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1797964097
gnomAD v4: 7-117479724-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479724G>C , CM000669.2:g.117479724G>C GRCh38
NC_000007.13:g.117119778G>C , CM000669.1:g.117119778G>C GRCh37
NC_000007.12:g.116907014G>C NCBI36
NG_016465.4:g.18941G>C , LRG_663:g.18941G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-191+30G>C ENSP00000417012.1:n.-191+30G>C
ENST00000673785.1:c.-406+13893G>C ENSP00000501235.1:n.-406+13893G>C
ENST00000446805.1:c.-191+30G>C ENSP00000417012.1:n.-191+30G>C
ENST00000546407.1:n.166+3916G>C
XM_011515751.1:c.143+379G>C XP_011514053.1:n.143+379G>C
XM_011515752.1:c.143+379G>C XP_011514054.1:n.143+379G>C
XM_011515753.1:c.-191+30G>C XP_011514055.1:n.-191+30G>C
XM_011515754.1:c.-519+30G>C XP_011514056.1:n.-519+30G>C
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